Lec 6 Management of Neurologic and MSK conditions Flashcards

1
Q

how is the MACS assessment normally preformed? (Manual ability classification system)

A

By asking someone who knows the child and how that child typically performs

(not by direct observation)

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2
Q

What kind of assessment can categorize a 4-18 year old with CPs ability to handle objects in everyday activities

A

MACS- Manual Ability Classification System

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3
Q

Child handles objects easily and successfully, maybe has some limitation of speed and accuracy but does not restrict independence

A

MACS 1

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4
Q

What is the distinction between MACS 1 and MACS 2

A

MACS 1 children might have speed/accuracy difficulty with small/heavy/fragile objects…

MACS 2 have speed/accuracy difficulties with all objects - these children try to simplify handling of objects (example: use surface for support instead of using 2 hands to handle the object)

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5
Q

Child handles most objects but with reduced quality or speed of movement

A

MACS 2

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6
Q

Child handles objects w/ difficulty and needs help to prepare or modify activity

A

MACS 3

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7
Q

What is the distinction between MACS 2 and MACS 3

A

MACS 3 cannot preform certain activities bc their degree of dependence is related to environmental context

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8
Q

Child handles a limited selection of easily managed objects in adapted situations

A

MACS 4

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9
Q

Child does not handle objects and is severely limited to preform even simple actions

A

MACS 5

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10
Q

What is the distinction between MACS 4 and MACS 5

A

Children at level 4 may preform part of an activity with continuous assistance

children at level 5 might at best only be able to do a simple movement in special situations like pushing a button

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11
Q

What measure is designed to describe functional mobility in children with CP between the ages of 4-18

A

FMS Functional Mobility Scale

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12
Q

What is unique about the FMS?

A

Gives you the freedom to score mobility across 3 different distances (mobility in home, mobility at school, mobility in wider community)

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13
Q

FMS scores:

A

6: Independent on all surfaces
5:independent on level surfaces
4: uses sticks (1 or 2)
3: Uses crutches
2: uses walker or frame
1: uses wheelchair
C: Crawls
N: Does not apply

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14
Q

FMS score 5

A

Independent on level surfaces

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15
Q

FMS score 2

A

Uses walker or frame

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16
Q

FMS Score 3

A

Uses crutches

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17
Q

FMS score 1

A

Uses wheelchair

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18
Q

the GMFM-88(Original) is valid for what ages?

What about the new GMFM-66?

A

5 months to 16 years
5 years to 16 years

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19
Q

T or F: The GMFM has been validated for not only CP, but also downsyndrome

A

T

note: emerging evidence to use it for TBI, SMA, OI, and other diagnosis

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20
Q

What dimensions are included in the GMFM?

How is it scored?

A

Lying+rolling

Sitting

Crawling/kneeling

standing

walking/running/jumping

Scores:
0: does not initiate task
1: initiates task
2: partially completes task
3: Completes task
NT: not tested

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21
Q

The GMFM is appropriate for those with motor skills at or below ______________________

A

at or below those of a 5 year old child without any motor disability

So even though it’s valid for up to 16 years, you should only use it for children w/ skills of a 5 year old

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22
Q

What equipment do you need for the GMFM

A

Mat, Bench, Access to stairs (at least 5 steps)

and space for a 4.5 meter run

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23
Q

Which should be used for testing children that are using ambulatory aids/ orthosis/shoes: GMFM-66 or GMFM 88

A

GMFM- 88,

the GMFM-66 is only for barefoot

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24
Q

Which is quicker to administer: GMFM-66 or GMFM-88

A

GMFM-66 is shorter and it doesn’t require all items to be assessed to get accurate score

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25
Between the GMFM-66 and the GMFM-88, which is better for documenting change over time
GMFM-66 because the items are ordered by level of difficulty
26
How long does it take to administer the GMFM-88
45-60 minutes
27
Spina Bifida precautions
Latex allergy Hydrocephalus Knowledge of shunt malfunctions Knowledge of tethered cord Be aware of sudden changes in foot posture or bowel/bladder function
28
myelomeningocele precautions
**monitor for scoliosis** d/c strength/sensation impaired B/B Poor motor control dc mobility deficits dependent on level of injury
29
Pt w/ Spina Bifida is experiencing headaches, vomiting, lethargy, and irritability
possible shunt malfunction
30
Pt w/ spina bifida is experiencing vision changes, decreased school performance, and cognitive changes
possible shunt malfunction
31
What is the incidence of shunt malfunction?
15%
32
What are signs of tethered cord syndrome
weakness/numbness tremors or spasms in leg muscles changes in way the feet look loss of B/B control
33
For children with down syndrome, radiographs should be taken _____________
between 3-5 years old to look for OA instability (present in 15%)
34
Downsyndrome complications
**Cardiac, Endocrine** (mainly hypothyroid) issues Heart defects Cervical instability OA instability
35
What is Part B of the Individuals with Disability Education Improvement Act
Established school aged services for students 3-21 with disabilities
36
What is the IEP for a student under Part B of the IDEA act
IEP= individualized education program, legally binding document developed **annually** for students note: Also the PTE- permission to evaluate, and the NOREP: notice of recommended education placement (which outlines the type of classroom and programming the student will receive)
37
Which part of the IDEA act is for birth-3 years old
Part C, develops early intervention for infants and toddlers with disabilities
38
What is the IFSP from the IDEA part C how often is it reviewed
Individualized family service plan for those receiving early intervention educated atleast once per year and reviewed every 6 months
39
What is the Individuals with Disabilities Education Improvement Act (2004)
Federal law provides financial assistance to states to implement early intervention program
40
What does section 504 of the rehabilitation act of 1973 say
Provides students, who do not require special education, services like physical therapy if they are considered to have a disability
41
What does the ADA act do?
Federal law prohibits discrimination against those with disabilities
42
T or F: you can use diagnostic ultrasound on Epiphysial plates
T NOT therapeutic ultrasound
43
What is developmental biomechanics
Effects of forces on MSK system throughout lifespan
44
What are the 3 key tissues of growth
connective tissue bones muscles
45
What are the 2 types of connective tissue:
Dense ordinary CT- tendons and ligaments Cartilage- found at the site of articulating joints
46
a common complication of tendon regeneration is the development of _______________ between the tendon and the surrounding tissue
fibrous adhesions
47
Bones, cartilage, and muscle are derived from the ______ layer of embryonic development
mesoderm layer
48
Epiphysial plates vs epiphysial lines:
Lines occur when the plates have fused and come together, growth no longer possible
49
What is heuter-volkman principle
growth plates produce increased growth in response to tension, decreased growth in response to excessive compression
50
How is skeletal maturity measured
SMI (skeletal maturity indicators), done by taking an xray of the left wrist, hand and fingers
51
what is Risser sign?
Percent of ossification of the iliac epiphysis indicates how much growth you have left example: can be used to see what kind of treatment is appropriate for a childs scoliosis by deciding how much conservative therapy can help
52
The posterior fontanelle closes: The anterior fontanelle closes:
1-2 months 7-18 months (cranial orthosis wont work past 18 months)
53
What is OI?
Osteogenesis Imperfecta- Genetic disorder characterized by bones that break easy
54
How should we educate parents for handling infants with OI?
Carry with widespread hands over head, shoulders, and bottom diaper change done by lifting buttocks, NOT ANKLES No twisting or pulling on bodyparts (caution with shoes and braces)
55
Should you MMT a child with OI?
May not be possible, you can do it they can tolerate it If they can tolerate: do on the mid-shaft of the bone NOT at the end! NO isolated trunk extension/flexion to assess core strength
56
A child with OI has a joint contracture, should we develop an orthosis with an aggressive stretch?
F, need extreme caution when dealing with contractures for pts with OI
57
OI type 1 OI type 2
Mildest type OI type 2: intrauterine fractures and infant death
58
OI type 3: OI type 4:
3: Severe! fractures at birth, causes short stature. 4: mild to moderate severity
59
What kind of drug do patients with OI take to prevent bone loss
biphosphonates
60
What symptoms of hydrocephalus are unique to children
Rapid head growth (fontanelles not closed yet) Bulging fontanelles (if they are not closed) Developmental delays
61
What are the clinical characteristics of Osteogenesis imperfecta
Hyperlaxity of ligaments Fragile skin Poor thermoregulation Blue sclerae Issues with teeth (dentinogenesis imperfecta)
62
Symptoms of hydrocephalus in infants
Bulging/tense soft spots, downward looking eyes, enlarged head, high pitched crying, seizures, problems w/ feedings
63
Symptoms of hydrocephalus in children/adults
Headache, vision changes, B/B, balance, Nausea and vomiting, decline in job or school performance, poor coordination, difficulty sleeping
64
Symptoms of hydrocephalus in older adults
Difficulty walking, slow shuffling, memory problems, dementia, tremor, balance
65
What is hydromyelia
Condition where the central canal of spinal cord is abnormally widened, creating a cavity filled with CSF
66
What are symptoms of hydromyelia
Headache Loss of temperature sensitivity Muscle stiffness Scoliosis Weakness in arms and leg Sensory loss/ severe pain in neck/arms
67
What percent ossified is a grade 3 Riser sign?
50-75%